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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 8 (1970), S. 643-648 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 2717-2724 
    ISSN: 0887-6266
    Keywords: tussah silk ; fibroin ; methanol treatment ; α-helix structure ; β-sheet structure ; dynamic mechanical analysis ; thermomechanical analysis ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal response of tussah (Antheraea pernyi) silk fibroin films treated with different water-methanol solutions at 20°C was studied by means of dynamic mechanical (DMA) and thermomechanical (TMA) analyses as a function of methanol concentration and treatment time. The DMA curves of α-helix films (treated with ≥80% v/v methanol for 2 min and 100% methanol for 30 min) showed the sharp fall of storage modulus at about 190°C, and the loss peak in the range 207-213°C. The TMA curves were characterized by a thermal shrinkage at 209-211°C, immediately followed by an abrupt extension leading to film failure. Both storage and loss modulus curves significantly shifted upwards for β-sheet films, obtained by treatment with ≤60% methanol for 30 min. The loss peak exhibited a maximum at 236°C. Accordingly, the TMA shrinkage at above 200°C disappeared. The films broke beyond 330°C, failure being preceded by a broad contraction step. Intermediate DMA and TMA patterns were observed for the other solvent-treated films. The loss peak shifted to higher temperature (219-220°C), and a minor loss modulus component appeared at about 230°C. This coincided with the onset of a plateau region in the storage modulus curve. The TMA extension-contraction events in the range 200-300°C weakened, and the samples displayed a final broad contraction (peak temperature 326-338°C) before breaking. The DMA and TMA response of these films was attributed to partial annealing by solvent treatment, which resulted in the formation of nuclei of β-sheet crystallization within the film matrix. The increased thermal stability was probably due to the small β-sheet crystals formed, which acted as high-strength junctions between adjacent random coil and α-helix domains. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 2717-2724, 1998
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 15 (1977), S. 1675-1683 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal behavior of films of amorphous silk fibroin in the random-coil conformation has been investigated in the temperature range 25-220°C by differential scanning calorimetry (DSC), thermal expansion, dynamic mechanical measurements, x-ray diffraction, and infrared spectroscopy. As the temperature is raised, water is lost up to about 100°C. Intramolecular and intermolecular hydrogen bonds are broken between 150 and 180°C. The glass transition is observed at 173°C by DSC. The random-coil→β-form transition accompanied by reformation of hydrogen bonds takes place above 180°C. Thermally induced crystallization to the β-form crystals starts at about 190°C.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Asymmetric selective (or stereoelective) polymerization of racemic 1,2-diphenylethyl methacrylate (DPEMA) with ethylmagnesium bromide (EtMgBr)-(-)-sparteine catalyst was studied in toluene at -78°C. In the polymerization (S) enantiomer was consumed preferentially and the enantiomeric excess of initially polymerized (S) enantiomer was consumed preferentially and the enantiomeric excess of initially polymerized DPEMA was greater than 90%. Optically pure (R) monomer was recovered at about 70% polymer yield. Poly(DPEMA) obtained with EtMgBr-(-)-sparteine complex was highly isotactic. It was found in the polymerization of optically active DPEMA that optical rotation of poly(DPEMA) was dependent on the tacticity and that isotactic and syndiotactic poly(DPEMA)s showed opposite optical rotations. Circular dichroism spectra of the optically active polymers were measured.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 291-299 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymorphism in nylon-12 film, which appears on casting from a phenol-ethanol solution, has been investigated by x-ray diffraction and infrared absorption. The casting temperature was varied from 30 to 130°C and the ambient atmospheric pressure from 50 to 760 Torr. Casting at 30°C gives only the α form, while casting above 90°C yields only the γ form. At intermediate temperatures, both α and γ forms are obtained, with the γ content increasing as the casting temperature and/or the rate of evaporation of solvent are increased. The ethanol component of the casting solvent appears to act only as a melting-point depressant for phenol. In contrast, nylon-6 film cast from the same solvent system between 30 and 160°C gives only the α form. It is proposed that the difference in polymorphism of nylons-12 and -6 is caused by differences in molecular flexibility due to the length of the methylene chain.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 1413-1419 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal behavior of α nylon-12 film cast from a phenol-ethanol mixture has been studied by differential scanning calorimetry. Polymorphism has been analyzed by x-ray diffraction. The γ form exhibits a single endothermic melting peak in the thermogram, whereas the α form exhibits double peaks. Samples with mixed α and γ forms show double peaks at the same positions and the area ratio changes in accordance with the amounts of the two forms. The appearance of the γ peak, even for the α sample, is explained by recrystallization to the γ form after melting of the α form. The melting point of α nylon-12 is ca. 173°C, which is lower by 6-7° than that of the γ form. Once the α or γ sample has been melted and then cooled, its heating thermogram shows a small peak before the appearance of the main peak. The small peak seems to be due to incomplete and/or smaller crystallites formed during cooling. Heat treatment below the melting point of α nylon-12 is effective in transforming the α form to the γ form, probably via a melt-recrystallization process.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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